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dc.contributor.authorAye, Irving
dc.contributor.authorGong, Sung
dc.contributor.authorAvellino, Giulia
dc.contributor.authorBarbagallo, Roberta
dc.contributor.authorGaccioli, Francesca
dc.contributor.authorJenkins, Benjamin J
dc.contributor.authorKoulman, Albert
dc.contributor.authorMurray, Andrew
dc.contributor.authorStephen Charnock-Jones, D
dc.contributor.authorSmith, Gordon
dc.date.accessioned2022-06-16T08:26:07Z
dc.date.available2022-06-16T08:26:07Z
dc.date.issued2022-06-15
dc.identifier.issn2399-3642
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/338150
dc.description.abstractPlacental function and dysfunction differ by sex but the mechanisms are unknown. Here we show that sex differences in polyamine metabolism are associated with escape from X chromosome inactivation of the gene encoding spermine synthase (SMS). Female placental trophoblasts demonstrate biallelic SMS expression, associated with increased SMS mRNA and enzyme activity. Polyamine depletion in primary trophoblasts reduced glycolysis and oxidative phosphorylation resulting in decreased acetyl-coA availability and global histone hypoacetylation in a sex-dependent manner. Chromatin-immunoprecipitation sequencing and RNA-sequencing identifies progesterone biosynthesis as a target of polyamine regulated gene expression, and polyamine depletion reduced progesterone release in male trophoblasts. The effects of polyamine depletion can be attributed to spermine as SMS-silencing recapitulated the effects on energy metabolism, histone acetylation, and progesterone release. In summary, spermine metabolism alters trophoblast gene expression through acetyl-coA biosynthesis and histone acetylation, and SMS escape from X inactivation explains some features of human placental sex differences.
dc.description.sponsorshipThe work was supported by a Centre for Trophoblast Research Next Generation Fellowship to Irving Aye and the NIHR Cambridge Biomedical Research Centre (BRC, United Kingdom; G1100221).
dc.publisherSpringer Science and Business Media LLC
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titlePlacental sex-dependent spermine synthesis regulates trophoblast gene expression through acetyl-coA metabolism and histone acetylation.
dc.typeArticle
dc.publisher.departmentDepartment of Obstetrics And Gynaecology
dc.date.updated2022-05-31T15:19:27Z
prism.publicationNameCommun Biol
dc.identifier.doi10.17863/CAM.85560
dcterms.dateAccepted2022-05-24
rioxxterms.versionofrecord10.1038/s42003-022-03530-6
rioxxterms.versionVoR
dc.contributor.orcidAye, Irving [0000-0003-3400-5005]
dc.contributor.orcidGong, Sung [0000-0001-5796-4423]
dc.contributor.orcidAvellino, Giulia [0000-0002-7413-0217]
dc.contributor.orcidGaccioli, Francesca [0000-0001-7178-8921]
dc.contributor.orcidJenkins, Benjamin J [0000-0003-0038-9709]
dc.contributor.orcidKoulman, Albert [0000-0001-9998-051X]
dc.contributor.orcidMurray, Andrew [0000-0002-0929-9315]
dc.contributor.orcidStephen Charnock-Jones, D [0000-0002-2936-4890]
dc.contributor.orcidSmith, Gordon [0000-0003-2124-0997]
dc.identifier.eissn2399-3642
rioxxterms.typeJournal Article/Review
pubs.funder-project-idCambridge University Hospitals NHS Foundation Trust (CUH) (146281)
cam.issuedOnline2022-06-15
cam.depositDate2022-05-31
pubs.licence-identifierapollo-deposit-licence-2-1
pubs.licence-display-nameApollo Repository Deposit Licence Agreement


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Except where otherwise noted, this item's licence is described as Attribution 4.0 International